Sterilization Validation and Routine Operation Handbook (2001)

Radiation

Anne Booth (Autor)

Buch | Hardcover

170 Seiten

2017
CRC Press (Verlag)
978-1-138-50673-2 (ISBN)

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The validation and radiation sterilization process for biomaterials and medical devices requires careful planning to ensure regulatory compliance followed by precise accuracy in execution and documentation. This in-depth guide details all steps from prevalidation planning to final report and ongoing monitoring and control. Sterilization Validation & Routine Operation Handbook: Radiation provides a framework for the validation and routine operation of an irradiation sterilization process. The guidance presented complies with ANSI/AAMI/ISO 11137: 1994, Sterilization of health care product-Requirements for validation and routine control-Radiation sterilization and the newly published AAMI substantiation of 25 kGy using VDmax procedure. The author discusses methods to aid in comprehending the requirements in these standards. She also provides practical procedures for the validation and routine monitoring and control of specific gamma and electron beam radiation sterilization processes.

Background chapters provide needed information on radiation sterilization technologies, sterilization microbiology, validation approaches and working with a radiation sterilization contractor. Much of the information in this new book is presented in convenient tables and charts, with diagrams and other schematics that simply illustrate appropriate validation methodologies. Sterilization Validation & Routine Operation Handbook: Radiation brings together in one resource information scattered throughout many documents and will be useful to all those involved in the sterilization of medical materials, drugs and devices.

Anne F.Booth President Booth Scientific, Inc An experienced quality and sterilization professional with an in-depth knowledge of quality systems and sterilization process design, validation, cycle development and routine operation; of environmental monitoring and control and regulatory compliance issues. Detailed knowledge of FDA QSR requirements (21 CFR 820 and 210/211), as well as ISO 13485, ICH, EU MDD and Canadian requirements. Experienced in project and laboratory management. Skilled in process design and validation for a wide variety of medical devices, packaging, and pharmaceutical raw materials. Good troubleshooting, auditing and time management skills. Track record of significant contributions to improved operating efficiency, cost reduction, and profit enhancement. Specialties: sterilization design and validation, quality systems, environmental monitoring, microbiology evaluations and testing, auditing

Rationale for Validating Sterilization Processes. Characterization of Radiation Processes. Contract Sterilization. Prevalidation Planning. Microbiological Considerations. Sterilization Support Testing. The Validation Protocol. Outline of the Sterilization Validation. Final Report. Routine Monitoring and Control. Appendices. Glossary. Bibliography.

Erscheinungsdatum	19.12.2017
Reihe/Serie	CRC Press Revivals
Verlagsort	London
Sprache	englisch
Maße	150 x 222 mm
Gewicht	470 g
Themenwelt	Schulbuch / Wörterbuch
	Medizin / Pharmazie ► Medizinische Fachgebiete ► Laboratoriumsmedizin
	Naturwissenschaften ► Biologie
	Recht / Steuern ► EU / Internationales Recht
	Recht / Steuern ► Privatrecht / Bürgerliches Recht ► Medizinrecht
	Technik ► Umwelttechnik / Biotechnologie
ISBN-10	1-138-50673-7 / 1138506737
ISBN-13	978-1-138-50673-2 / 9781138506732
Zustand	Neuware